US5032298A - Low-molecular weight acrylate-acrylamide copolymers, their manufacture and use to prevent deposition of salts from aqueous media - Google Patents

Low-molecular weight acrylate-acrylamide copolymers, their manufacture and use to prevent deposition of salts from aqueous media Download PDF

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US5032298A
US5032298A US07/103,330 US10333087A US5032298A US 5032298 A US5032298 A US 5032298A US 10333087 A US10333087 A US 10333087A US 5032298 A US5032298 A US 5032298A
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copolymer
weight
monomers
copolymer according
acrylamide
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Claude Roque
Alain Ribba
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IFP Energies Nouvelles IFPEN
Manufacture de Produits Chimiques Protex SARL
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    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
    • C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
    • C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
    • C02F5/12—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/04—Acids; Metal salts or ammonium salts thereof
    • C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/52—Amides or imides
    • C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • C08F220/56—Acrylamide; Methacrylamide
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02—Well-drilling compositions
    • C09K8/04—Aqueous well-drilling compositions
    • C09K8/06—Clay-free compositions
    • C09K8/12—Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24—HEATING; RANGES; VENTILATING
    • F24T—GEOTHERMAL COLLECTORS; GEOTHERMAL SYSTEMS
    • F24T10/00—Geothermal collectors
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F28—HEAT EXCHANGE IN GENERAL
    • F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
    • F28F19/00—Preventing the formation of deposits or corrosion, e.g. by using filters or scrapers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/10—Geothermal energy
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00—Earth boring, well treating, and oil field chemistry
    • Y10S507/927—Well cleaning fluid

Definitions

  • the present invention concerns low molecular weight copolymers of acrylic acid or at least partially salified acrylic acid and acrylamine, their process of manufacture and their use to prevent the formation of deposits of on the walls of oil or geothermal equipment from aqueous systems containing dissolved salts.
  • the invention relates to a process for inhibiting depositions resulting from incompatibilities of the injection and field waters and/or from their destabilization.
  • Nonlimitative applications of the invention are those relating to oil or geothermal industries, bottom and surface equipments used in the domain of wall injectivity and productivity and generally those using industrial aqueous systems.
  • anionic polymers and copolymers have been used as agents for inhibiting inorganic deposits, as disclosed for example, in U.S. Pat. Nos. 4,072,607, 4,175,100; and 4,518,511. Generally, their weight distribution ranges from 500 to 25,000. Some of them may have a weight distribution in the range of from 3,000 to 300,000, which is controlled, as disclosed in U.S. Pat. No. 4,143,222.
  • U.S. Pat. No. 4,072,607 discloses the preparation of a acrylate-acrylamide copolymer mixture in molar proportions from about 20:1 to 1:1 having a molecular weight ranging from 500 to 12,000, with a distribution that such at least 60% of said copolymer has a molecular weight of from 500 to 2,000, at least 10% a molecular weight of from 4,000 to 12,000 and the remainder has a molecular weight of from 2,000 to 4,000, these distributions being determined by exclusion chromatography.
  • This copolymer is prepared by polymerizing acrylamide monomer in the presence of an initiator and a chain transfer agent, the obtained polyacrylamide being partially hydrolyzed to sodium acrylate.
  • a chain transfer agent introduced during polymerization, first in a proportion of 3% and then in a proportion of 16% with respect to acrylamide, the above-mentioned weight distribution is observed.
  • U.S. Pat. Nos. 3,665,035 and 3,756,257 disclose the use, as a crystallization prevention agent in the treatment of oil wells, of a polymer composition obtained by reacting at 24° C., in an inert solvent such as water, 80-90 parts by weight of acrylic acid, as single monomer, with 7-15 parts by weight of thioglycolic acid, as a chain transfer agent, and 1.5-5 parts by weight of ammonium persulfate, as a radical initiator.
  • the acrylic acid obtained has an average molecular weight of from 500 to 1,000.
  • copolymers of high molecular weight are difficult to solubize and hence difficult to use in the prevailing conditions of deep fields with highly salted water (e.g., 150-350 g/l salt content), high temperature and pressure (e.g., 120°-150° C., 100-400 bars) and had a lower inhibiting activity in the above-mentioned thermodynamic conditions. Moreover, it has been observed that the inhibition effect of these products was very short (a few hours) even under thermodynamic conditions of low severity.
  • a first object of the invention is to provide a new copolymer composition of acrylic acid and/or acrylate-acrylamide of very low molecular weight, useful for preventing precipitation and/or formation of crystalline deposits onto the surfaces in contact with incompatible water.
  • Another object is to provide a process for manufacturing such a copolymer composition.
  • Another object of the invention is to provide a process involving the use of products soluble in mixtures of salted waters (particularly having a salt content of 350 g/l or more) and whose activity level is high under the severe thermodynamic conditions prevailing in deep fields.
  • Another object is to provide a process for injecting inhibiting agents soluble in the salted water to be injected (e.g., sea-water and water from water-bearing strata).
  • inhibiting agents soluble in the salted water to be injected e.g., sea-water and water from water-bearing strata.
  • Still another object is to provide a process for inhibiting the crystalline growth of the deposits, under the thermodynamic conditions of surface as well as those of the very deep reservoirs.
  • a further object is the use of an inhibitor solution whose properties are maintained over periods compatible with the length of the oil treatments during the production stage, as well as during, the treatment at the surface which may be performed on-site at a far distance from the production place.
  • the present invention overcomes the above-mentioned disadvantages and fulfills these objects. It concerns an anionic copolymer or copolymer composition comprising acrylic acid and acrylamide in respective proportions by weight ranging from 95:5 to 25:75, advantageously from 90:10 to 50:50.
  • the distribution of the molecular weight of said copolymer, determined by exclusion analytic chromatography, is such that at least 60% of the weight molecular weights are lower than 500. Its polydispersity is at most 3 and advantageously at most 2.
  • the invention also concerns a copolymer composition or anionic copolymers comprising recurrent units derived from acrylic acid, at least partly as alkaline salts and acrylamide, the values of the ratio by weight, the distribution of molecular weights and the polydispersity being defined as above.
  • the acrylate alkaline salts are advantageously sodium acrylate, potassium acrylate and ammonium acrylate, either alone or as a mixture.
  • a copolymer composition according to the invention is a mixture of copolymers, as defined above, having in the molecule such a number of recurrent units (for example, from 2 to 10) that the average molecular weight corresponds to the above definition according to the invention.
  • the invention also concerns a process for manufacturing a copolymer, characterized as the reaction product of the following four constituents:
  • the operation is advantageously conducted in a medium comprising an inert solvent, at a temperature from 60° to 120° C., preferably from 70° to 100° C.
  • the total amount of said monomers in proportion by weight to said medium is from 4 to 15%.
  • the chain transfer agent is used in an amount of 10-20% by weight and the catalyst in amount of 2-8% by weight in proportion to said monomers, the first and second monomers being in respective proportions by weight from 95:5 to 25:75, so as to obtain a product comprising a mixture of the desired copolymer with the solvent.
  • the reaction is exothermic and the exothermicity is controlled by cooling the reaction mixture.
  • the reaction is performed in solution and any inert solvent or system of inert solvents adapted to solubilize the charge constituents or not to substantially react with the charge or the copolymer composition formed may be used. Water is particularly advantageous as a solvent for the sake of economy and convenience.
  • the proportion of monomers in the polymerization medium is low. This characteristic, together with exothermicity control, are favorable to the formation of a copolymer of low molecular weight.
  • the copolymerization reaction may be completed by adding to said solvent-copolymer product a further catalyst amount of 0.5-4% by weight in proportion to said monomers, the reaction being allowed to continue so that substantially all the monomers are used up.
  • the copolymerization may be conducted in several successive steps instead of a single step. Accordingly, the involved amount of constituents is divided into substantially equal aliquot parts, a first copolymerization reaction is performed under the above-define conditions and in proportions of constituents, so as to form the solvent-copolymer product.
  • a first copolymerization reaction is performed under the above-define conditions and in proportions of constituents, so as to form the solvent-copolymer product.
  • another copolymerization reaction is performed by adding to the solvent-copolymer product of the preceding reaction an aliquot part of said first and second monomers, an aliquot part of the chain transfer agent and an aliquot part of catalyst, each of the successive copolymerization reactions being performed substantially under the conditions and with the proportions of the various constituents previously defined for the first reaction steps.
  • a low charge of acrylic acid, acrylamide, chain transfer agent and catalyst can be added to the system in the above-mentioned amounts and weight ratios in the single-stage process, and the multi-stage process can be repeated with the addition of further successive charges until the copolymer composition reaches a high level of active matter.
  • the reaction will be repeated 3 to 10 times so as to obtain the desired concentration of final product. For example, a proportion of active matter of 52% has been obtained after 10 successive additions of charge.
  • the chain transfer agent is preferably thioglycolic acid. It is advantageously used in an amount of from 5 to 30%, preferably 12-15% by weight in proportion to all the monomers.
  • Radical initiator catalysts are, for example, hydrogen peroxide or an alkali metal persulfate, for example, a sodium, potassium or ammonium persulfate.
  • alkali metal persulfate for example, a sodium, potassium or ammonium persulfate.
  • the above-mentioned persulfates are particularly convenient in the domain of high reaction temperatures.
  • Ammonium persulfate is generally used in an amount of 2-8% by weight, preferably 3-5% by weight in proportion to the total amount of monomers.
  • the monomers copolymerize at a temperature of from 60° to 120° C., preferably in the range of from 70° to 100° C. They are generally used at the available commercial purity degree in an amount of 4-15%, preferably 6-12% by weight in proportion to the copolymerization medium to which they are added.
  • the reaction time at each stage is generally short, usually from 10 to 60 min. per reaction.
  • the copolymer neutralization makes the obtained product less corrosive. It is generally performed at a pH of from 3 to 9, depending on the desired degree of neutralization, with such a neutralizing agent as, for example, sodium and potassium hydroxides ammonium hydroxide, mono-and polyalkanolamines, and at a temperature generally at most equal to 70° C.
  • the neutralization agent may be slowly added so as to control the temperature and the dissolution. A substantial formation of vapor is thus avoided.
  • the two-step manufacture of the copolymers according to the invention comprises:
  • the two-step process of the invention is advantageous since, after the copolymers have been injected, their amide sites remain in part potentially hydrolyzable and their secondary salification by contact with the reservoir cations becomes possible, so that the inhibiting properties of the products according to the invention, prepared according to said operating mode and injected for example into the producing well, remain substantially undamaged over periods which may reach several weeks.
  • the surface equipment through which the so-treated fluids will have to flow may thus be protected over distances of several kilometers by this persistent effect of the inhibiting properties.
  • the process of the invention has the purpose of at least partly preventing the deposition, on the walls of oil or geothermal or industrial equipment, of salts from an aqueous medium, containing in particular alkali and/or alkaline-earth metals, flowing through said equipment.
  • the molecular weight distribution of said copolymer, determined by exclusion analytic chromatography is such that at least 60% of the weight molecular weights are lower than 500.
  • This process offers the advantage of inhibiting the incrustation in the walls of the deposits already present or formed from aqueous media in the conditions prevailing at the surface as well as in those of very deep reservoirs, e.g. at 30°-250° C. under 1 to 500 bars and with a water salt content up to about 350 g/l.
  • FIGS. 1 to 4 of the accompanying drawings diagrammatically showing exclusion chromatograms.
  • Exclusion chromatography is one of the most efficient methods for analyzing the molecular weight distributions of the copolymers according to the invention.
  • the eluant is formed of 0.5 M NaCl in water and the analysis is performed at 1.0 ml/mn.
  • the molecules of larger size, hence of higher molecular weight, cannot penetrate the pores and are thus excluded, i.e. eluted at first, whereas the smaller molecules which penetrate the pores of the particles are retained and are finally the last to be eluted. Then, with reference to known molecular weights, the obtained chromatogram can be calibrated.
  • elution volume Ve (ml) (corresponding to a scale of molecular weights) is plotted as the abscissa and the relative amount of said molecular weights plotted as the ordinate, for different acrylamide-sodium acrylate balances or constitutions.
  • elution volumes of 28 ml, 29 ml, 29.5 ml and 31.5 ml correspond to respective molecular weights of 1 000, 500 and 400 for polyoxyethylene and 62 for ethylene glycol, eluted with water.
  • Table I hereinafter gives the essential characteristics of the obtained chromatograms.
  • the weight molecular weight Mw and the number molecular weight Mn are defined as follows: ##EQU1##
  • the percentage of copolymers having a particular molecular weight range, e.g. lower than 500, is determined by integration in a known-per-se manner, of the exclusion chromatograms.
  • the inhibitor may be introduced in dry state into one of the waters of the aqueous system, preferably into the soft or salted injection water, optionally formed of a water mixture. It may also be introduced into a commercial solution comprising for example 50-60% of active matter. For sake of convenience, the inhibitor may also be introduced from more diluted solutions whose concentration may be, for example, as low as 20 grams per liter. These solutions may be prepared in advance, which constitutes a substantial advantage in exploitation for generalized injections since the solutions may be stored and their ageing (from a few minutes to about ten days) does not change the inhibiting activity of the copolymer (and is sometimes advisable).
  • 1 to 200 ppm (parts per million) of active matter according to the invention can be introduced into the aqueous medium. Excellent results are obtained, particularly for the activity of crystalline growth inhibition (above-defined) substantially equal to 100%, under very severe thermodynamic conditions of the field, with a 15-50 ppm concentration of active matter.
  • the inhibition efficiency also depends on the copolymer constitution, i.e. on the acrylate/acrylamide ratio by weight.
  • an inhibition activity A is defined by gravimetry as: ##EQU2## wherein m 1 and m 2 are the weights of deposits obtained by admixing the waters respectively in the absence and in the presence of inhibitor, these deposits being recovered under the same conditions.
  • the previously recovered field and injection waters may be admixed in any proportion but preferably in a ratio corresponding to the so-called critical mixture, as defined below.
  • they are brought to thermodynamic conditions similar to those prevailing in deep oil reservoirs for each water mixture ratio.
  • the water incompatibility may result particularly in the formation of deposits of alkaline-earth sulfate, mainly barium or calcium sulfate, carbonates, sulfides and phosphates of the alkali or alkaline-earth type.
  • the precipitated salts are recovered by filtration under differential pressure, dried and weighed. The results are plotted as a substantially parabolic gravimetry curve of water incompatibility from which can be determined, around its maximum, the critical water mixture corresponding to maximum deposits.
  • the inhibitor according to the invention is introduced in the above-mentioned thermodynamic conditions.
  • a curve of the activity versus the inhibitor concentration giving the range of optimum inhibitor concentration required to obtain an inhibition activity of substantially 100%, may thus be determined.
  • the inhibitor at said optimum concentration may thus be determined.
  • the process according to the invention copes with the difficulties resulting from the incompatibility of various water mixtures within a ionic strength range from 0.05 to 6.5 and a pH range from 8.5 to 5.0, these limits being not compulsory.
  • the inhibitor according to the invention may also be dissolved into additives commonly used in oil production, for example demulsifying agents, anticorrosive agents, bactericide agents, antifoam agents, etc...
  • reactant amounts are expressed as parts by weight.
  • a stirred reactor equipped with a reflux condenser, a thermometer and an addition funnel, is charged with 2700 parts of deionized water and 3 parts of DTPA Masquol (sodium salt of diethylene triamine pentacetic acid).
  • the reactor is heated to about 75° C. and, at said temperature, fed with 306 parts of acrylic acid, 102 parts of acrylamide and 49 parts of thioglycolic acid (acting as a chain transfer agent).
  • a solution of 12.6 parts of ammonium persulfate in 114 parts of deionized water is introduced into the reactor. An exothermic reaction takes place. The temperature increases from 75° to 95° C.
  • the exothermicity is controlled so as to prevent the temperature to increase above 95° C.
  • the reaction is rapid and lasts 15-20 minutes.
  • the mixture is cooled to 90° C. and a solution of 4 parts of ammonium persulfate in 30 parts of deionized water is again charged into the reactor.
  • the reaction is continued for 30 minutes and the reaction mixture is cooled to 75° C.
  • This procedure is repeated 9 times successively by introducing at each time into the reaction mixture 306 parts of acrylic acid, 102 parts of acrylamide, 49 parts of thioglycolic acid, then a solution of 12.6 parts of ammonium persulfate in 114 parts of deionized water and, after completion of the exothermic reaction, a solution of 4 parts of ammonium persulfate into 30 parts of deionized water.
  • the temperature is maintained for 2 additional hours at 90° C. after a solution of 9 parts of ammonium persulfate in 70 parts of deionized water has been added for reducing to a maximum extent the residual free monomers.
  • the mixture is then cooled to 60° C. and 1000 parts of flaky soda are slowly added thereto so as to neutralize it to a pH from 5.5 to 6.
  • the mixture is cooled to 20° C., and, by mere dilution, the [, product is adjusted to standards of active matter, pH and viscosity.
  • the obtained aqueous solution of 25:75 by weight copolymer of acrylamide and sodium acrylate at 52% concentration has a pH of about 5.5-6 and a viscosity of about 0.3 to 0.5 Pa.s at 20° C. with the molecular weight distribution shown in FIG. 2.
  • Example 1 is repeated in the same conditions except that the monomers consist of 204 parts of acrylic acid of 204 parts of acrylamide.
  • a 50-50 acrylate-acrylamide copolymer is obtained which is defined by the exclusion chromatogram of FIG. 4.
  • the admixture is conducted at 120° C. under 200 bars and with a reaction time of 4 hours in the presence of the gaseous and liquid hydrocarbons of the field.
  • the deposits After opening of the reactor, the deposits are recovered by filtration under differential pressure, dried and weighed, the obtained deposit amount m 1 being necessary to calculate the inhibition activity.
  • the required concentrations for 100% activity are compared for copolymers comprising 25% of acrylamide and 75% of sodium acrylate according to the invention and copolymers of higher molecular weight having the same constitution (25% acrylamide - 75% sodium acrylate) introduced, according to example 3, in a injection water C of Albian type admixed with a field water D of Cambrian type in the critical mixture ratio of 40% C - 60% D.
  • the composition of these waters is given in tables VI and VII.
  • the results of example 4 are reported in table V.
  • copolymers of different salt contents are prepared (acrylamide-ammonium acrylate copolymer or acrylamide-potassium acrylate copolymer).
  • a 100% inhibition activity is obtained with substantially the same inhibitor concentrations as in example 3, for identical copolymer constitutions.
  • the inhibitor (25% acrylamide - 75% sodium acrylate copolymer) is introduced into sea-water as in example 3 from a solution containing 10g of active matter per liter of injection water and after ageing for 10 days.
  • the 100% inhibition activity is obtained with an inhibitor concentration substantially identical to that of example 3.

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US07/103,330 1986-10-02 1987-10-01 Low-molecular weight acrylate-acrylamide copolymers, their manufacture and use to prevent deposition of salts from aqueous media Expired - Lifetime US5032298A (en)

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FR8613862 1986-10-02
FR8613862A FR2604712B1 (fr) 1986-10-02 1986-10-02 Copolymere acrylate acrylamide a bas poids moleculaire et procede pour empecher au moins en partie la formation de depot de sels issus de milieux aqueux

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EP (1) EP0266234B1 (fr)
JP (1) JP2673428B2 (fr)
CN (1) CN1011038B (fr)
CA (1) CA1321673C (fr)
DE (1) DE3764606D1 (fr)
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US20050049327A1 (en) * 2003-09-02 2005-03-03 Vladimir Jovancicevic Drag reducing agents for multiphase flow
US9102767B2 (en) 2009-03-25 2015-08-11 Total Raffinage Marketing Low molecular weight (meth)acrylic polymers, free of sulphur-containing, metallic and halogenated compounds and with low residual monomer content, method for preparing the same and uses thereof
WO2021106148A1 (fr) 2019-11-28 2021-06-03 Kurita Water Industries Ltd. Copolymères anioniques appropriés comme inhibiteurs d'entartrage

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JP4496666B2 (ja) * 2001-05-16 2010-07-07 東亞合成株式会社 重合体水溶液の製造方法
CN108993318B (zh) * 2015-12-15 2021-04-27 沙特阿拉伯石油公司 用于石油升级的超临界反应器系统和工艺

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US3756257A (en) * 1971-10-04 1973-09-04 Magna Corp Acrylic composition for water treatment and process for making same
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US4359483A (en) * 1980-02-27 1982-11-16 Japan Atomic Energy Research Institute Process for producing a multi-layered slow release composite
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050049327A1 (en) * 2003-09-02 2005-03-03 Vladimir Jovancicevic Drag reducing agents for multiphase flow
WO2005021690A1 (fr) * 2003-09-02 2005-03-10 Baker Hughes Incorporated Agents de reduction de resistance de frottement dans un ecoulement polyphasique
US9102767B2 (en) 2009-03-25 2015-08-11 Total Raffinage Marketing Low molecular weight (meth)acrylic polymers, free of sulphur-containing, metallic and halogenated compounds and with low residual monomer content, method for preparing the same and uses thereof
WO2021106148A1 (fr) 2019-11-28 2021-06-03 Kurita Water Industries Ltd. Copolymères anioniques appropriés comme inhibiteurs d'entartrage
WO2021106710A1 (fr) 2019-11-28 2021-06-03 Kurita Water Industries Ltd. Copolymères anioniques appropriés comme inhibiteurs d'entartrage pour les dépôts contenant des sulfures

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ES2018562B3 (es) 1991-04-16
CN87106624A (zh) 1988-07-13
JPS63183907A (ja) 1988-07-29
DE3764606D1 (de) 1990-10-04
NO170548C (no) 1992-10-28
EP0266234A1 (fr) 1988-05-04
EP0266234B1 (fr) 1990-08-29
NO874106L (no) 1988-04-05
DZ1129A1 (fr) 2004-09-13
JP2673428B2 (ja) 1997-11-05
NO170548B (no) 1992-07-20
CN1011038B (zh) 1991-01-02
CA1321673C (fr) 1993-08-24
TNSN87109A1 (fr) 1990-01-01
NO874106D0 (no) 1987-09-30
FR2604712B1 (fr) 1988-12-30
FR2604712A1 (fr) 1988-04-08

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